Skip to main content
Log in

Genetic analyses of Tattered, an X-linked dominant, developmental mouse mutation

  • Original Contributions
  • Published:
Mammalian Genome Aims and scope Submit manuscript

Abstract

Tattered (Td) is an X-linked dominant mouse mutation that causes prenatal lethality in affected males. To map the locus, we analyzed 199 normal male and affected female progeny from a backcross of Td and Mus castaneus. Pedigree analysis of these animals suggests a gene order of cen-DXWas70-(Td, DXMit26, Gatal, Tcfe3)-(Cybb, Otc)-tel, where Tcfe3 is a transcription factor homologous to a gene involved in the murine microphthalmia (mi) mutation [Hodgkinson et al. Cell 74, 395–404, 1993]. To evaluate Tcfe3 as a candidate for Td, heterozygous tattered females were crossed to xid males to obtain females in which >95% of B cells expressed genes solely from the Td X Chromosome (Chr). Fluorescent activated cell sorting (FACS) analysis and Western blotting of isolated splenocytes from Td/xid double heterozygotes rule out Tcfe3 as a likely candidate for the Td mutation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Blair, H.J., Boyd, Y. (1994). Positioning of 14 simple sequence repeat loci relative to markers on the gene-based map of the mouse X chromosome. Mouse Genome 92, 127–129.

    Google Scholar 

  • Blair, H.J., Reed, V., Laval, S.H., Boyd, Y. (1994a). New insights into the man-mouse comparative map of the X chromosome. Genomics 19, 215–220.

    Google Scholar 

  • Blair, P.J., Carpenter, D.A., Godfrey, V.L., Russell, L.B., Rinchik, E.M. (1994b). The scurfy (sf) mutation is tightly linked to Gatal/Tfe3 on the proximal X chromosome. Mamm. Genome 5, 652–654.

    Google Scholar 

  • Brown, S.D.M., Avner, P., Boyd, Y., Chapman, V., Rastan, S., Sefton, L., Thomas, J.D., Herman, G.E. (1993). Mouse X Chromosome. Mamm. Genome 4 (Suppl.), S269-S281.

    Google Scholar 

  • Cattanach, B.M. (1982a). A new X-linked mutation. Mouse News Lett 66, 61–62.

    Google Scholar 

  • Cattanach, B.M. (1982b). Location of tattered (Td). Mouse News Lett. 67, 19.

    Google Scholar 

  • Chirgwin, J.M., Przybyla, A.E., MacDonald, R.J., Rutter, W.J. (1979). Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18, 5294–5299.

    Google Scholar 

  • Cremin, S.M., Greer, W.L., Bodok-Nutzati, R., Schwartz, M., Peacocke, M., Siminovitch, K.A. (1993). Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 region. Hum. Genet. 92, 250–253.

    Google Scholar 

  • Derry, J.M.J., Ochs, H.D., Francke, U. (1994). Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell 78, 635–644.

    Google Scholar 

  • Faust, C.J., Herman, G.E. (1991). Physical mapping of the loci Gabra3, DXPas8, CamL1, and Rsvp in a region of the mouse X chromosome homologous to human Xq28. Genomics 11, 154–164.

    Google Scholar 

  • Glover, T.W., Verga, V., Rafael, J., Barcroft, C., Gorski, J.L., Bawle, E.V., Higgins, J.V. (1993). Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323. Hum. Mol. Genet. 2, 1717–1718.

    Google Scholar 

  • Herman, G.E., Walton, S.J. (1990). Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata. Genomics 7, 307–312.

    Google Scholar 

  • Hodgkinson, C.A., Moore, K.J., Nakayama, A., Steingrimsson, E., Copeland, N.G., Jenkins, N.A., Arnheiter, H. (1993). Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 74, 395–404.

    Google Scholar 

  • Kantor, A.B., Stall, A.M., Adams, A., Herzenberg, L.A., Herzenberg, L.A. (1992). Differential development of progenitor activity for three B cell lineages. Proc. Natl. Acad. Sci. USA 89, 3320–3324.

    Google Scholar 

  • Laval, S.H., Boyd, Y. (1993). Partial inversion of gene order within a homologous segment on the X Chromosome. Mamm. Genome 4, 119–123.

    Google Scholar 

  • Nahm, M.H., Paslay, J.W., Davie, J.M. (1983). Unbalanced X chromosome mosaicism in B cells of mice with X-linked immunodeficiency. J. Exp. Med. 158, 920–931.

    Google Scholar 

  • Pevny, L., Simon, M.C., Robertson, E., Klein, W.H., Tsai, S.-F., D'Agati, V., Orkin, S.H., Constantini, F. (1991). Erythroid differentiation in chimaeric mice blocked by a targeted gene mutation for transcription factor GATA1. Nature 349, 257–260.

    Google Scholar 

  • Rawlings, D.J., Saffran, D.C., Tsukada, S., Largaespada, D.A., Grimaldi, J.C., Cohen, L., Mohr, R.N., Bazan, F., Howard, M., Copeland, N.G., Jenkins, N.A., Witte, O.N. (1993). Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID mice. Science 261, 358–361.

    Google Scholar 

  • Roman, C., Lohn, L., Calame, K. (1991). Creation of a trans-dominant negative form of transcription activator in TFE3 by differential splicing. Science 254, 94–97.

    Google Scholar 

  • Roman, C., Matera, A.G., Cooper, C., Artandi, S., Blain, S., Ward, D.C., Calame, K. (1992). mTFE3, an X-linked transcriptional activator containing basic helix-loop-helix and zipper domains, utilizes the zipper to stabilize both DNA binding and multimerization. Mol. Cell. Biol. 12, 817–827.

    Google Scholar 

  • Sybert, V.P. (1994). Incontinentia pigmenti nomenclature. Am. J. Hum. Genet. 55, 209–211.

    Google Scholar 

  • Thomas, J.D., Sideras, P., Edward Smith, C.I., Vorechovsky, I., Chapman, V., Paul, W.E. (1993). Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes. Science 261, 355–358.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Merrell, K., Gonzales, J.C., Wells, S. et al. Genetic analyses of Tattered, an X-linked dominant, developmental mouse mutation. Mammalian Genome 6, 291–294 (1995). https://doi.org/10.1007/BF00352419

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00352419

Keywords

Navigation